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MAP kinase mediates epidermal growth factor- and phorbol ester-induced prostacyclin formation in cardiomyocytes

Published in Journal of Molecular and Cellular Cardiology. 1998, vol. 30, no. 5, p. 933-45
Abstract We studied the role of protein kinase C (PKC) and mitogen-activated protein kinase (MAPK) in epidermal growth factor (EGF)-induced prostacyclin (PGI2) production in cultured, spontaneously-beating neonatal ventricular rat cardiomyocytes. To this purpose, the effect of EGF on cardiomyocyte MAPK phosphorylation, MAPK activity and PGI2-production were investigated, and compared to those induced by the PKC activator 4 beta phorbol 12-myristate 13-acetate (PMA). Both EGF (0.1 microM) and PMA (0.1 microM) induced the rapid and reversible phosphorylation of 42 KDa-MAPK in ventricular cardiomyocytes, responses that were accompanied by transient increases in MAPK activity (190-230% of control values within 5 min), and two- to three-fold increases in PGI2 formation. The tyrosine kinase inhibitors lavendustin (1 microM) and genistein (10 microM) strongly inhibited EGF-induced MAPK activation and PGI2-formation, but had no effect on PMA-stimulated responses. Experiments with the PKC inhibitor CGP 41251 (1 microM) or with PKC-downregulated cells demonstrated that in contrast to the PMA-stimulated responses, EGF-induced MAPK activation and PGI2-production were PKC-independent processes. Investigating the role of MAPK in EGF- and in PMA-promoted PGI2-formation, we found that the MAPK-inhibitor 6-thioguanine (500 microM), as well as the MAPK-kinase-inhibitor PD98059 (50 microM) abolished both EGF- and PMA-stimulated PGI2-production in cardiomyocytes. Our results indicate that MAPK-activation is at the basis of both growth factor receptor and PKC-dependent eicosanoid-formation in ventricular cardiomyocytes, where EGF-induced prostaglandin-production takes place via a PKC-independent pathway.
Keywords Analysis of VarianceAnimalsCalcium-Calmodulin-Dependent Protein Kinases/physiologyCells, CulturedEnzyme ActivationEpidermal Growth Factor/pharmacologyEpoprostenol/biosynthesisHeart Ventricles/cytology/drug effects/metabolismPhosphorylationRatsRats, WistarTetradecanoylphorbol Acetate/pharmacology
PMID: 9618234
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BRACONI QUINTAJE, Silvia et al. MAP kinase mediates epidermal growth factor- and phorbol ester-induced prostacyclin formation in cardiomyocytes. In: Journal of Molecular and Cellular Cardiology, 1998, vol. 30, n° 5, p. 933-45. doi: 10.1006/jmcc.1998.0657 https://archive-ouverte.unige.ch/unige:1162

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Deposited on : 2009-03-17

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